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CNS-For MBBS/BDS theory lecture
Antiepileptic agents
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Linda Fowler
Please find the power point on Management of antipsychotic overdose. I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
Management of antipsychotic overdose
Management of antipsychotic overdose
sunil kumar daha
antiparkinsonism
13.antiparkinsonian drugs, antiepileptics & alcohol
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Dr.Manish Kumar
SECOND & THIRD GENERATION ANTIPSYCHOTIC mechanism of actionmechanism of side effectmanagment of side effect BY DR WASIM UNDERGUIDANCE OF DR SANJAY JAIN First generation=typical antipsychoticaka conventionalprimary pharmacological property of D2 antagonistSecond generation=atypical antipsychoticlow EPS and good for negative symptomsThird generation=aripiprazole metabolic friendly MECHANISM OF ACTION 1) serotonin dopamine antagonists 4)serotonin partial agonist MECHANISM OF SIDE EFFECT Serotonin-2C, muscarinic-3, and histamine-1 receptors as well as receptors X identified are all hypothetically linked to cardiometabolic risk. antagonism of serotonin-2C and histamine-1 receptors is associated with weight gain, while antagonism atmuscarinic-3 receptors can impair insulin regulation. An unknown receptor X may be involved in the rapid production of insulin resistance and may also rapidly cause elevated fasting plasma triglyceride levels in some patients who experience increased cardiometabolic risk on certain atypical antipsychotics Atypical antipsychotic and risk for weight gain.FDA and experts agree on three tiers of risk Atypical antipsychotic and cardiometabolic risk.FDA and experts disagree on one versus three teirs of risk Metabolic friendly antipsychotic.Low- risk agents for weight gain and cardiacmetabolic illness. Monitoring and Managment Baseline investigations : Family h/o diabetes BMI Fasting TG levels (also monitored throughout treatment) If raised : consider switching to another agent +/- lifestyle changes For obese/ prediabetic/ diabetic pts : Monitor BP Fasting glucose Waist circumference (before and after Rx) Be vigilant for DKA/HHS Sedation ARIPIPRAZOLE KNOWN AS THIRD GENERATION ANTIPSYCHOTIC THANK YOU
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Anant Rathi
this class is in brief for undergraduate understanding and examination
Class anti-epileptics
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Recommandé
CNS-For MBBS/BDS theory lecture
Antiepileptic agents
Antiepileptic agents
Dr.Arka Mondal
Toxicology
Toxicology
Linda Fowler
Please find the power point on Management of antipsychotic overdose. I tried to present it on understandable way and all the contents are reviewed by experts and from very reliable references. Thank you
Management of antipsychotic overdose
Management of antipsychotic overdose
sunil kumar daha
antiparkinsonism
13.antiparkinsonian drugs, antiepileptics & alcohol
13.antiparkinsonian drugs, antiepileptics & alcohol
Dr.Manish Kumar
SECOND & THIRD GENERATION ANTIPSYCHOTIC mechanism of actionmechanism of side effectmanagment of side effect BY DR WASIM UNDERGUIDANCE OF DR SANJAY JAIN First generation=typical antipsychoticaka conventionalprimary pharmacological property of D2 antagonistSecond generation=atypical antipsychoticlow EPS and good for negative symptomsThird generation=aripiprazole metabolic friendly MECHANISM OF ACTION 1) serotonin dopamine antagonists 4)serotonin partial agonist MECHANISM OF SIDE EFFECT Serotonin-2C, muscarinic-3, and histamine-1 receptors as well as receptors X identified are all hypothetically linked to cardiometabolic risk. antagonism of serotonin-2C and histamine-1 receptors is associated with weight gain, while antagonism atmuscarinic-3 receptors can impair insulin regulation. An unknown receptor X may be involved in the rapid production of insulin resistance and may also rapidly cause elevated fasting plasma triglyceride levels in some patients who experience increased cardiometabolic risk on certain atypical antipsychotics Atypical antipsychotic and risk for weight gain.FDA and experts agree on three tiers of risk Atypical antipsychotic and cardiometabolic risk.FDA and experts disagree on one versus three teirs of risk Metabolic friendly antipsychotic.Low- risk agents for weight gain and cardiacmetabolic illness. Monitoring and Managment Baseline investigations : Family h/o diabetes BMI Fasting TG levels (also monitored throughout treatment) If raised : consider switching to another agent +/- lifestyle changes For obese/ prediabetic/ diabetic pts : Monitor BP Fasting glucose Waist circumference (before and after Rx) Be vigilant for DKA/HHS Sedation ARIPIPRAZOLE KNOWN AS THIRD GENERATION ANTIPSYCHOTIC THANK YOU
Second and third generation antipsychotics
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Parkinson diseases
Parkinson diseases
N K
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Typical antipsychotics
Typical antipsychotics
Anant Rathi
this class is in brief for undergraduate understanding and examination
Class anti-epileptics
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Management of adverse effect of antipsychotics 1
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sadaf89
Some info on the mechanism of action of typical vs. atypical antipsychotics.
Overview of the Mechanism of Typical vs Atypical Antipsychotics
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Christiane Riedinger
Adverse effects antipsychotics dr ali
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OSMAN ALI MD
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Shah Parind
Prepared for a presentation at Jaffna Medical Association's weekly clinical meetings. This is an overview of Neuroleptic malignant syndrome.
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Brian Piper
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ANTI PSYCHOTIC AGENTS / ANTI PSYCHOTIC DRUGS / DRUG USED IN THE TREATMENT OF PSYCHOSIS for B.Pharm and Pharm.D
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Kameshwaran Sugavanam
Anticonvulsants are a diverse group of pharmacological agents used in the treatment of epileptic seizures. Charles Locock commented in the Lancet on his use of potassium bromide in 15 cases of "hysterical" epilepsy in young women. The next development was the serendipitous discovery of the anticonvulsant properties of phenobarbital by Alfred Hauptmann in 1912. This predated by more than 20 years the screening of potential therapeutic agents against "electrical seizures" in cats by Houston Merritt and Tracy Putnam. The result was the launching of phenytoin in 1938. Next came primidone, ethosuximide, carbamazepine and valproic acid, all of which can be regarded as first generation antiepileptic drugs (AEDs). Shortly after their synthesis, the benzodiazepines were rapidly recognised as having anticonvulsant activity. The modern era focused on the systematic screening of many thousands of compounds against rodent seizure models under the Anticonvulsant Drug Development Program in the US. This resulted in the global licensing, in chronological order, of vigabatrin, zonisamide, oxcarbazepine, lamotrigine, felbamate, gabapentin, topiramate, tiagabine, levetiracetam, pregabalin and lacosamide.
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Tendances
newer antipsychotic iloperidone, by anant kumar rathi
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Some info on the mechanism of action of typical vs. atypical antipsychotics.
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OSMAN ALI MD
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Bhudev Global
This seminar was delivered to 2nd year pharmacy students as part of 2 lectures for a pharmacology & toxicology class. This material accompanies Goodman & Gilman's (12e) chapter 22.
Pharmacotherapies for parkinsons disease
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Brian Piper
the Pharmacology of schizophrenia.
Antipsychotic agents
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Steve Wilkins
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Antipsychotics I
Antipsychotics I
Brian Piper
Psychosis and Anti-psychotic Drugs
Antipsychotics
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Chetan Rastogi
Parkinson’S Disease
Parkinson’S Disease
mohammed sediq
ANTI PSYCHOTIC AGENTS / ANTI PSYCHOTIC DRUGS / DRUG USED IN THE TREATMENT OF PSYCHOSIS for B.Pharm and Pharm.D
ANTI PSYCHOTIC AGENTS / ANTI PSYCHOTIC DRUGS / DRUG USED IN THE TREATMENT OF ...
ANTI PSYCHOTIC AGENTS / ANTI PSYCHOTIC DRUGS / DRUG USED IN THE TREATMENT OF ...
Kameshwaran Sugavanam
Anticonvulsants are a diverse group of pharmacological agents used in the treatment of epileptic seizures. Charles Locock commented in the Lancet on his use of potassium bromide in 15 cases of "hysterical" epilepsy in young women. The next development was the serendipitous discovery of the anticonvulsant properties of phenobarbital by Alfred Hauptmann in 1912. This predated by more than 20 years the screening of potential therapeutic agents against "electrical seizures" in cats by Houston Merritt and Tracy Putnam. The result was the launching of phenytoin in 1938. Next came primidone, ethosuximide, carbamazepine and valproic acid, all of which can be regarded as first generation antiepileptic drugs (AEDs). Shortly after their synthesis, the benzodiazepines were rapidly recognised as having anticonvulsant activity. The modern era focused on the systematic screening of many thousands of compounds against rodent seizure models under the Anticonvulsant Drug Development Program in the US. This resulted in the global licensing, in chronological order, of vigabatrin, zonisamide, oxcarbazepine, lamotrigine, felbamate, gabapentin, topiramate, tiagabine, levetiracetam, pregabalin and lacosamide.
Anti epileptics-pharmacology and guidelines
Anti epileptics-pharmacology and guidelines
Navya devireddy
Anti-Parkinsonism Drugs / Drugs Used in the treatment of Parkinson's Disease as per the PCI syllabus
Anti-Parkinsonism Drugs / Drugs Used in the treatment of Parkinson's Disease
Anti-Parkinsonism Drugs / Drugs Used in the treatment of Parkinson's Disease
Kameshwaran Sugavanam
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Dr Namrata Mohan
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Rawalpindi Medical College
Tendances
(20)
Iloperidone
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Overview of the Mechanism of Typical vs Atypical Antipsychotics
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Adverse effects antipsychotics dr ali
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9. antipsychotics
9. antipsychotics
Emergencies Caused By Psychiatric Drugs
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Both Alzheimer’s disease and Parkinson’s disease are diseases of the brain. Both may cause forgetfulness. However, the similarities end there. In fact, researchers believe that even the memory disorder that results from Parkinson’s is distinct from the memory disorder that Alzheimer’s causes. One main difference between the diseases is how they affect the body: Alzheimer’s disease primarily affects memory. In advanced stages, the disease also impairs motor functions. Parkinson’s disease primarily affects movement and coordination. In advanced stages, it may impair memory and other cognitive functions.
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